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Data / Medical devices / Vinyl Patient Examination Glove / United States

FDA-registered makers of Vinyl Patient Examination Glove in the United States: 11 establishments

11 establishments in the United States are registered with the FDA to make Vinyl Patient Examination Glove (product code LYZ). 10 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device
Vinyl Patient Examination Glove
Product code
LYZ
Country
United States

Makers of Vinyl Patient Examination Glove in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesComplaint file establishment, Specification developer11July 17, 2021000api.fda.gov
K2 Health ProductsBrooklyn, NY, United StatesSpecification developer6June 17, 2013000api.fda.gov
Ansell Healthcare Products LLCReno, NV, United StatesManufacturer, Specification developer4January 31, 2014000api.fda.gov
Mexpo International, Inc.Union City, CA, United StatesManufacturer4March 2, 2012000api.fda.gov
Bay MedicalBrisbane, CA, United StatesSpecification developer1February 8, 2007000api.fda.gov
Lifeline First Aid LLCLake Oswego, OR, United StatesRepackager or relabeler, Specification developer1November 13, 2003000api.fda.gov
Mayer LaboratoriesBerkeley, CA, United StatesRepackager or relabeler, Specification developer1May 5, 1999000api.fda.gov
PM Gloves, Inc.Chino, CA, United StatesComplaint file establishment, Specification developer1March 2, 2012000api.fda.gov
Sna Safehealth Solutions Inc.Monrovia, CA, United StatesComplaint file establishment, Specification developer1February 5, 2016000api.fda.gov
SW Technologies Inc.Union City, CA, United StatesManufacturer1January 8, 2004000api.fda.gov
A-1 Creative Packaging LLCFort Atkinson, WI, United StatesContract manufacturer0000api.fda.gov

Updated November 3, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.